Viewing Study NCT06504108



Ignite Creation Date: 2024-10-26 @ 3:35 PM
Last Modification Date: 2024-10-26 @ 3:35 PM
Study NCT ID: NCT06504108
Status: NOT_YET_RECRUITING
Last Update Posted: None
First Post: 2024-06-18

Brief Title: Full Pulpotomy Procedure of Permanent Molar Teeth of Adults Using Calcium Silicate-based Sealer Material
Sponsor: None
Organization: None

Study Overview

Official Title: Evaluation Of The Efficacy Of Using Calcium-Silicate Based Sealers As A Pulp Capping Material After Adult Pulpotomy An In-vivo Study
Status: NOT_YET_RECRUITING
Status Verified Date: 2024-07
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: No
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: None
Brief Summary: This clinical study aims to assess the efficacy of using calcium silicate based sealer as a capping material after complete removal of coronal pulp tissue The study will evaluate both the clinical and radiographic changes
Detailed Description: Root canal treatment has always been considered the first line of treatment for carious teeth with symptomatic irreversible pulpitis for a long time However after the evolution of calcium silicate based materials a more conservative option which is pulpotomy began to gain reliability especially that it preserves the vitality of the radicular pulp clinically simpler less time-consuming and more cost-effective compared to conventional root canal treatment

In this study the investigators assess the clinical and radiographic success rate of using calcium silicate based sealer as a pulp capping material in permanent molars after pulpotomy

For the best of the investigators39 knowledge there is no available clinical data on the use of calcium-silicate based sealers as a pulp capping material in pulpotomy of permanent molars with symptoms of irreversible pulpitis

Study Oversight

Has Oversight DMC: None
Is a FDA Regulated Drug?: None
Is a FDA Regulated Device?: None
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: None
Is an FDA AA801 Violation?: None